Canonical Allele Identifier: CA658843403

Gene:

Linked Data

• dbSNP Id: rs1388728707
• MyVariant Identifiers: chr10:g.101861491del (hg19) ; chr10:g.100101734del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.100101734del , CM000672.2:g.100101734del	GRCh38
NC_000010.10:g.101861491del , CM000672.1:g.101861491del	GRCh37
NC_000010.9:g.101851481del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_946245.1:n.185+5497del